Last synced on 25 April 2025 at 11:05 pm

Cortera Spinal Fixation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221403
510(k) Type
Traditional
Applicant
Surgalign Spine Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/2022
Days to Decision
95 days
Submission Type
Summary

Cortera Spinal Fixation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221403
510(k) Type
Traditional
Applicant
Surgalign Spine Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/2022
Days to Decision
95 days
Submission Type
Summary